Use this URL to cite or link to this record in EThOS:
Title: The influence of drug use and apolipoprotein E on HIV related disease of the central nervous system
Author: Arango-Viana, Juan Carlos
Awarding Body: University of Edinburgh
Current Institution: University of Edinburgh
Date of Award: 2002
Availability of Full Text:
Access from EThOS:
Full text unavailable from EThOS. Please try the link below.
Access from Institution:
Aims: i) To determine the contribution of host factors such as drug use (DU) and apolipoprotein E (ApoE) genotype in the development of HIVE and HAD. ii) To investigate some histological changes relevant to HAD in drug users with different ApoE genotypes. Methods: Genotyping for ApoE was carried out in 312 individuals who were divided into five groups. Group I consisted of 64 normal controls, Group II consisted of 82 HIV negative drug users, Group III consisted of 38 presymptomatic HIV positive drug users (pre AIDS), Group IV consisted of 84 drug users with AIDS, Group V consisted of non drug users with AIDS (6 haemophiliacs and 38 men who have sex with men (MSM). Results: Analyses showed that the frequency of ApoE e2 allele in the HIV positive drug users (Groups III and IV taken together, n=122) was 14.3%. In contrast, the frequency for the ApoE e2 in groups I (n=64) and II (n=82) was 5.4% in each group and 8.2% in normal Scottish population (group VI, n=400). These differences were significant (X2=7.017, p<0.008, and X2=7.580, p<0.006, respectively). At the same time, the ApoE e3 allele for groups III and IV was found to be under represented when compared to the Scottish population (X2=9.695, p<0.0002). More detailed comparisons between different genotype subsets within the groups all gave results supportive of the main finding of ApoE e2 over representation. Group V showed no difference in ApoE genotype from the general population. CD4 and CD8 counts were found to be significantly higher in group IV compared with Group V. 53.9% Group IV individuals had CD4 counts above 50th percentile, in contrast to only 21.5% in individuals in group V (X2= 11.242, p<0.001). For CD8, 48.8% of the group IV cases had counts above the 50th percentile, while only 23.1% of group V were above (X2=8.740, p<0.003). The ApoE e3 allele was found negatively associated with CD8 counts (X2=5.063, p<0.02), but the positive association of ApoE e2 allele with CD8 counts did not reach significance (X2=3.593, p<0.058). The histological change which was most strongly associated with dementia was HIVE (X2=14.977, p<0.0005). The association of ApoE alleles with HIVE showed that ApoE e2 and e3 alleles were significantly with HIVE (X2= 4.007, p<0.05 and X2=5.090, p<0.02 respectively), although the direction of the association with the ApoE e3 allele was negative.
Supervisor: Not available Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID:  DOI: Not available